Evidence map›Paper›PMID 28457994›Full record

ArticleJournal of clinical lipidology

Increase in acid sphingomyelinase level in human retinal endothelial cells and CD34

Nermin Kady, Yuanqing Yan, Tatiana Salazar, Qi Wang, Harshini Chakravarthy, Chao Huang, Eleni Beli, Svetlana Navitskaya, Maria Grant, Julia Busik

Open access · hybridAbstract read
In one paragraph

Article in Journal of clinical lipidology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.6field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 33 citations in OpenAlex.

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  8. Effects ofMolecules (Basel, Switzerland) · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Nermin KadyDepartment of Physiology, Michigan State University, East Lansing, MI, USA.
Yuanqing YanDepartment of Biostatistics, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Tatiana SalazarGenetics and Genomics Graduate Program, Department of Pharmacology and Therapeutics, University of Florida, Gainesville, FL, USA.
Qi WangDepartment of Physiology, Michigan State University, East Lansing, MI, USA.
Harshini ChakravarthyDepartment of Physiology, Michigan State University, East Lansing, MI, USA.
Chao HuangDepartment of Physiology, Michigan State University, East Lansing, MI, USA.
Eleni BeliDepartment of Ophthalmology, Indiana University School of Medicine, Indianapolis, USA.
Svetlana NavitskayaDepartment of Physiology, Michigan State University, East Lansing, MI, USA.
Maria GrantDepartment of Ophthalmology, Indiana University School of Medicine, Indianapolis, USA.
Julia BusikDepartment of Physiology, Michigan State University, East Lansing, MI, USA. Electronic address: busik@msu.edu.
Michigan State University · USIndiana University School of MedicineThe University of Texas MD Anderson Cancer Center · USUniversity of Florida · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
NITRIC OXIDE IN THE PATHOGENESIS OF DIABETIC RETINOPATHYR01EY012601 · NEI · UNIVERSITY OF FLORIDA · PI Julia V Busik, Maria Bartolomeo Grant · 1998 to 2026
$9.6M
Dyslipidemia and Diabetic RetinopathyR01EY016077 · NEI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI BUSIK, JULIA V · 2005 to 2025
$6.3M
Targeting the IGF-1 System in Retinal AngiogenesisR01EY007739 · NEI · UNIVERSITY OF FLORIDA · PI ABCOUWER, STEVEN F, GRANT, MARIA BARTOLOMEO · 1995 to 2015
$5.4M
LXR as a Novel Therapeutic Target in Diabetic RetinopathyR01EY025383 · NEI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BUSIK, JULIA V, GRANT, MARIA BARTOLOMEO · 2015 to 2024
$4.2M
NEI NIH HHS R01 EY007739NEI NIH HHS R01 EY012601NEI NIH HHS R01 EY016077NEI NIH HHS R01 EY025383NIDDK NIH HHS P30 DK020572
6 · The paper itself

Abstract

backgroundDiabetic retinopathy is a microvascular disease that results from retinal vascular degeneration and defective repair due to diabetes-induced endothelial progenitor dysfunction.

objectiveUnderstanding key molecular factors involved in vascular degeneration and repair is paramount for developing effective diabetic retinopathy treatment strategies. We propose that diabetes-induced activation of acid sphingomyelinase (ASM) plays essential role in retinal endothelial and CD34

methodsHuman retinal endothelial cells (HRECs) isolated from control and diabetic donor tissue and human CD34

resultsASM expression level was significantly increased in HRECs isolated from diabetic compared with control donor tissue, as well as CD34

conclusionCollectively, these findings support that diabetes-induced ASM upregulation has a marked detrimental effect on both retinal endothelial cells and CACs.

Indexed as

AgedAntigens, CD34Circadian RhythmDiabetic RetinopathyEndothelial CellsFemaleGene Expression Regulation, EnzymologicHumansMaleMiddle AgedNeovascularization, PathologicRetinaRetinal VesselsSphingomyelin Phosphodiesteraseacid sphingomyelinase-1Antigens, CD34Sphingomyelin PhosphodiesteraseAcid sphingomyelinaseCirculating angiogenic cellsDiabetic retinopathyRevascularization

Identifiers

PMID28457994
PMCPMC5492962
OpenAlexW2603855375

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.